Canonical Allele Identifier: CA85301687
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs1052186392
gnomAD v2: 3-143424745-G-C
gnomAD v3: 3-143705903-G-C
gnomAD v4: 3-143705903-G-C
MyVariant Identifiers: chr3:g.143424745G>C (hg19) chr3:g.143424745_143424746delinsCA (hg19) chr3:g.143705903G>C (hg38) chr3:g.143705903_143705904delinsCA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143705903G>C , CM000665.2:g.143705903G>C GRCh38
NC_000003.11:g.143424745G>C , CM000665.1:g.143424745G>C GRCh37
NC_000003.10:g.144907435G>C NCBI36
NG_017077.1:g.147629C>G
NG_017077.2:g.147629C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.534-12596C>G MANE Select ENSP00000320246.6:n.534-12596C>G
ENST00000316549.10:c.534-12596C>G ENSP00000320246.6:n.534-12596C>G
ENST00000474727.2:c.*145-12596C>G ENSP00000419090.2:n.*145-12596C>G
NM_173653.3:c.534-12596C>G NP_775924.1:n.534-12596C>G
XM_011512704.1:c.534-12596C>G XP_011511006.1:n.534-12596C>G
XM_011512704.3:c.534-12596C>G XP_011511006.1:n.534-12596C>G
XM_017006202.2:c.534-12596C>G XP_016861691.1:n.534-12596C>G
XM_017006203.1:c.183-12596C>G XP_016861692.1:n.183-12596C>G
NM_173653.4:c.534-12596C>G MANE Select NP_775924.1:n.534-12596C>G
Search 100 bp 5'
Search 100 bp 3'